TRIM77
gene geneOn this page
Summary
TRIM77 (tripartite motif containing 77, HGNC:34228) is a protein-coding gene on chromosome 11q14.3, encoding Tripartite motif-containing protein 77 (I1YAP6).
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in innate immune response and regulation of gene expression. Predicted to be active in cytoplasm.
Source: NCBI Gene 390231 — RefSeq curated summary.
At a glance
- GWAS associations: 2
- Clinical variants (ClinVar): 80 total
- MANE Select transcript:
NM_001146162
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:34228 |
| Approved symbol | TRIM77 |
| Name | tripartite motif containing 77 |
| Location | 11q14.3 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000214414 |
| Ensembl biotype | protein_coding |
| Entrez | 390231 |
Gene structure
Transcript identifiers
Ensembl transcripts: 2 — 2 protein_coding
ENST00000398290, ENST00000534392
RefSeq mRNA: 2 — MANE Select: NM_001146162
NM_001146162, NM_001271942
CCDS: CCDS60929
Canonical transcript exons
ENST00000398290 — 6 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001532516 | 89711410 | 89711505 |
| ENSE00001532518 | 89710299 | 89710709 |
| ENSE00003684119 | 89717379 | 89717872 |
| ENSE00003757720 | 89715158 | 89715180 |
| ENSE00003760169 | 89715890 | 89715987 |
| ENSE00003760260 | 89714192 | 89714422 |
Expression profiles
Bgee: expression breadth tissue_specific, 2 present calls, max score 57.57.
Top tissues by expression
129 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 57.57 | silver quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| sural nerve | UBERON:0015488 | 37.14 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 33.38 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| muscle tissue | UBERON:0002385 | 31.06 | gold quality |
| liver | UBERON:0002107 | 30.30 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.89 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| corpus callosum | UBERON:0002336 | 28.99 | gold quality |
| monocyte | CL:0000576 | 28.40 | gold quality |
| leukocyte | CL:0000738 | 28.33 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 27.50 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| blood | UBERON:0000178 | 26.04 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| placenta | UBERON:0001987 | 25.81 | gold quality |
| urinary bladder | UBERON:0001255 | 25.72 | gold quality |
| right lobe of liver | UBERON:0001114 | 24.84 | gold quality |
| muscle of leg | UBERON:0001383 | 24.74 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.12 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Paralogs (80): MID2 (ENSG00000080561), TRIM9 (ENSG00000100505), MID1 (ENSG00000101871), MEFV (ENSG00000103313), TRIM35 (ENSG00000104228), TRIM14 (ENSG00000106785), TRIM37 (ENSG00000108395), TRIM2 (ENSG00000109654), TRIM3 (ENSG00000110171), TRIM38 (ENSG00000112343), TRIM62 (ENSG00000116525), TRIM67 (ENSG00000119283), TRIM32 (ENSG00000119401), BSPRY (ENSG00000119411), TRIM25 (ENSG00000121060), TRIM6 (ENSG00000121236), TRIM24 (ENSG00000122779), TRIM51 (ENSG00000124900), TRIM28 (ENSG00000130726), TRIM21 (ENSG00000132109), TRIM5 (ENSG00000132256), TRIM22 (ENSG00000132274), TRIM47 (ENSG00000132481), TRIM45 (ENSG00000134253), TRIM29 (ENSG00000137699), TRIM54 (ENSG00000138100), PML (ENSG00000140464), TRIM65 (ENSG00000141569), TRIM43B (ENSG00000144010), TRIM43 (ENSG00000144015), TRIM7 (ENSG00000146054), TRIM41 (ENSG00000146063), TRIM50 (ENSG00000146755), TRIM4 (ENSG00000146833), TRIM55 (ENSG00000147573), TRIM48 (ENSG00000150244), TRIM36 (ENSG00000152503), TRIM11 (ENSG00000154370), TRIM74 (ENSG00000155428), TRIM42 (ENSG00000155890)
Protein
Protein identifiers
Tripartite motif-containing protein 77 — I1YAP6 (reviewed: I1YAP6)
All UniProt accessions (2): I1YAP6, S4R3H6
UniProt curated annotations — full annotation on UniProt →
Similarity. Belongs to the TRIM/RBCC family.
RefSeq proteins (2): NP_001139634, NP_001258871 (=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000315 | Znf_B-box | Domain |
| IPR001841 | Znf_RING | Domain |
| IPR001870 | B30.2/SPRY | Domain |
| IPR003877 | SPRY_dom | Domain |
| IPR003879 | Butyrophylin_SPRY | Domain |
| IPR013083 | Znf_RING/FYVE/PHD | Homologous_superfamily |
| IPR013320 | ConA-like_dom_sf | Homologous_superfamily |
| IPR017907 | Znf_RING_CS | Conserved_site |
| IPR018957 | Znf_C3HC4_RING-type | Domain |
| IPR043136 | B30.2/SPRY_sf | Homologous_superfamily |
| IPR050143 | TRIM/RBCC | Family |
Pfam: PF00097, PF00622
UniProt features (8 total): binding site 4, zinc finger region 2, chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-I1YAP6-F1 | 82.10 | 0.40 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Ligand- & substrate-binding residues (4): 93; 96; 115; 121
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 6 (showing top):
GOBP_DEFENSE_RESPONSE_TO_OTHER_ORGANISM, GOMF_ACYLTRANSFERASE_ACTIVITY, GOMF_AMINOACYLTRANSFERASE_ACTIVITY, GOMF_UBIQUITIN_LIKE_PROTEIN_LIGASE_ACTIVITY, chr11q14, GOBP_BIOLOGICAL_PROCESS_INVOLVED_IN_INTERSPECIES_INTERACTION_BETWEEN_ORGANISMS
GO Biological Process (2): regulation of gene expression (GO:0010468), innate immune response (GO:0045087)
GO Molecular Function (4): zinc ion binding (GO:0008270), ubiquitin protein ligase activity (GO:0061630), protein binding (GO:0005515), metal ion binding (GO:0046872)
GO Cellular Component (1): cytoplasm (GO:0005737)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| gene expression | 1 |
| regulation of macromolecule biosynthetic process | 1 |
| immune response | 1 |
| defense response to symbiont | 1 |
| transition metal ion binding | 1 |
| ubiquitin-protein transferase activity | 1 |
| ubiquitin-like protein ligase activity | 1 |
| binding | 1 |
| cation binding | 1 |
| intracellular anatomical structure | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
202 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TRIM77 | TRIM42 | Q8IWZ5 | 502 |
| TRIM77 | FAM153A | Q9UHL3 | 480 |
| TRIM77 | ZNF396 | Q96N95 | 473 |
| TRIM77 | TRIM52 | Q96A61 | 421 |
| TRIM77 | TRIM55 | Q9BYV6 | 419 |
| TRIM77 | TRIM59 | Q8IWR1 | 404 |
| TRIM77 | TRIM14 | Q14142 | 370 |
| TRIM77 | ANKRD20A4P | Q4UJ75 | 353 |
| TRIM77 | TRIM23 | P36406 | 348 |
| TRIM77 | TRIM67 | Q6ZTA4 | 324 |
| TRIM77 | TRIM47 | Q96LD4 | 322 |
| TRIM77 | FRG1 | Q14331 | 311 |
| TRIM77 | TRIM54 | Q9BYV2 | 293 |
| TRIM77 | TRIM56 | Q9BRZ2 | 293 |
| TRIM77 | TRIM74 | Q86UV6 | 278 |
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| TRIM77 | H2BC5 | psi-mi:“MI:0915”(physical association) | 0.400 |
BioGRID (1): HIST1H2BD (Proximity Label-MS)
ESM2 similar proteins: A0A3B3IT33, A6NCK2, A6NDI0, A6NGJ6, A6NI03, A6NLI5, C9J1S8, I1YAP6, K7N6K2, P0CI25, P0CI26, P15533, Q0PF16, Q1ACD5, Q1ACD6, Q1ACD7, Q1ACD8, Q2YEM8, Q2YEM9, Q2YEN0, Q2YEN2, Q3ZEE5, Q587N6, Q587N7, Q5BN31, Q5C8T6, Q5C8T8, Q5C8U1, Q5C8U3, Q5C8U4, Q5D7H7, Q5D7H8, Q5D7I0, Q5D7I1, Q5D7I2, Q5D7I3, Q5D7I5, Q5D7I6, Q5D7I9, Q5D7J0
Diamond homologs: A0A3B3IT33, A6NCK2, A6NDI0, A6NGJ6, A6NI03, A6NLI5, B0BLU1, C9J1S8, I1YAP6, O00478, O00481, O15344, O75677, O75678, O75679, O76064, P0CI25, P0CI26, P18892, P19474, P62603, P86448, P86449, Q13410, Q2HJ46, Q3C1V9, Q3TL54, Q4KLN8, Q5EBN2, Q5PQN2, Q5R4I2, Q5R996, Q61510, Q62556, Q6INS5, Q6MFY8, Q6UX41, Q6UXE8, Q6ZWI9, Q7T308
SIGNOR signaling
1 interactions.
| A | Effect | B | Mechanism |
|---|---|---|---|
| Ub:E2 | “up-regulates activity” | TRIM77 | ubiquitination |
Disease & clinical
Clinical variants and AI predictions
ClinVar
80 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 78 |
| Likely benign | 2 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
920 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 11:89711501:GGGAA:G | donor_gain | 1.0000 |
| 11:89711502:GGAAG:G | donor_gain | 1.0000 |
| 11:89711503:G:GT | donor_gain | 1.0000 |
| 11:89711503:G:T | donor_gain | 1.0000 |
| 11:89711506:G:GG | donor_gain | 1.0000 |
| 11:89711510:GCA:G | donor_gain | 1.0000 |
| 11:89711513:G:GG | donor_gain | 1.0000 |
| 11:89715884:TTGCA:T | acceptor_loss | 1.0000 |
| 11:89715885:TGCA:T | acceptor_loss | 1.0000 |
| 11:89715888:A:AG | acceptor_gain | 1.0000 |
| 11:89715888:A:G | acceptor_loss | 1.0000 |
| 11:89715888:AG:A | acceptor_gain | 1.0000 |
| 11:89715889:G:GG | acceptor_gain | 1.0000 |
| 11:89715889:G:GT | acceptor_loss | 1.0000 |
| 11:89715889:GG:G | acceptor_gain | 1.0000 |
| 11:89715889:GGA:G | acceptor_gain | 1.0000 |
| 11:89715889:GGAAT:G | acceptor_gain | 1.0000 |
| 11:89715985:GAG:G | donor_gain | 1.0000 |
| 11:89715986:AGG:A | donor_loss | 1.0000 |
| 11:89711502:GGAA:G | donor_gain | 0.9900 |
| 11:89711503:GAA:G | donor_gain | 0.9900 |
| 11:89715889:GGAA:G | acceptor_gain | 0.9900 |
| 11:89717137:G:GG | donor_gain | 0.9900 |
| 11:89717377:A:AG | acceptor_gain | 0.9900 |
| 11:89717378:G:GG | acceptor_gain | 0.9900 |
| 11:89717378:GT:G | acceptor_gain | 0.9900 |
| 11:89717378:GTGT:G | acceptor_gain | 0.9900 |
| 11:89711408:A:AG | acceptor_gain | 0.9800 |
| 11:89711409:G:GG | acceptor_gain | 0.9800 |
| 11:89717136:A:AG | donor_gain | 0.9800 |
AlphaMissense
3018 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 11:89717777:T:C | F420L | 0.975 |
| 11:89717779:T:A | F420L | 0.975 |
| 11:89717779:T:G | F420L | 0.975 |
| 11:89717747:T:C | F410L | 0.970 |
| 11:89717749:C:A | F410L | 0.970 |
| 11:89717749:C:G | F410L | 0.970 |
| 11:89717548:G:C | W343C | 0.964 |
| 11:89717548:G:T | W343C | 0.964 |
| 11:89717546:T:A | W343R | 0.959 |
| 11:89717546:T:C | W343R | 0.959 |
| 11:89717576:T:A | W353R | 0.957 |
| 11:89717576:T:C | W353R | 0.957 |
| 11:89717849:T:C | F444L | 0.947 |
| 11:89717851:C:A | F444L | 0.947 |
| 11:89717851:C:G | F444L | 0.947 |
| 11:89717586:G:A | G356E | 0.941 |
| 11:89717774:A:C | S419R | 0.936 |
| 11:89717776:C:A | S419R | 0.936 |
| 11:89717776:C:G | S419R | 0.936 |
| 11:89717645:T:C | F376L | 0.933 |
| 11:89717647:T:A | F376L | 0.933 |
| 11:89717647:T:G | F376L | 0.933 |
| 11:89717778:T:C | F420S | 0.929 |
| 11:89717547:G:C | W343S | 0.917 |
| 11:89717543:T:G | Y342D | 0.916 |
| 11:89710398:T:C | F34L | 0.912 |
| 11:89710400:T:A | F34L | 0.912 |
| 11:89710400:T:G | F34L | 0.912 |
| 11:89717578:G:C | W353C | 0.912 |
| 11:89717578:G:T | W353C | 0.912 |
dbSNP variants (sampled 300 via entrez): RS1000428182 (11:89717023 T>C), RS1000574934 (11:89712321 C>T), RS1001033665 (11:89718235 G>A,C,T), RS1001147514 (11:89717274 T>C), RS1001374289 (11:89717601 C>G), RS1001416271 (11:89711327 C>G), RS1002363746 (11:89712403 A>G), RS1002823162 (11:89712719 T>G), RS1003415426 (11:89714131 C>T), RS1004547371 (11:89717935 T>G), RS1004654719 (11:89711651 T>C), RS1004770625 (11:89711363 A>G), RS1005654692 (11:89713127 C>A), RS1005770807 (11:89712777 G>A), RS1007988683 (11:89708631 G>A,C)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
2 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST007998_24 | Intraocular pressure | 3.000000e-07 |
| GCST012020_222 | Serum metabolite levels | 6.000000e-20 |
EFO canonical traits (1, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0004695 | intraocular pressure measurement |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
1 total (human), top 1 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Aflatoxin B1 | decreases methylation | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.